Librela (bedinvetmab injection) is a monthly injectable monoclonal antibody, for which real-world drug experience data has ...

Zoetis (ZTS) announced that it has updated the U.S. label for Librela, following its submission of a supplement to the FDA. This supplement ...

Bayer has filed its mineralocorticoid receptor antagonist (MRA) finerenone as a treatment for a common form of heart failure ...

The FDA has approved a new type of painkiller that doesn't come with the risks of addiction and overdose associated with opioids.

A nasal spray that contains esketamine — a potent derivative of ketamine — can now be taken on its own to treat adults with ...

Yellow No. 5 is commonly used in brightly colored soda and candy, often to make them appear fresher and more appetizing. Yellow No. 6, which is also used in candy, may appear in salad dressings, ...

The US Food and Drug Administration (FDA) is urging manufacturers to revise labeling of transmucosal buprenorphine products to ease access to higher doses needed due to the rise of high-potency ...

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The best way to check if a product has the dye is to read the label printed on the package. The FDA requires companies to disclose when they use color additives in their ingredients list.

with the EU requiring warning labels on products containing it. This isn't the first time the FDA has wielded the Delaney Clause—similar actions were taken against certain synthetic flavors in ...

File photo: US Sen. Richard Blumenthal responds to a question during a news conference at Hartford HealthCare on Jan. 2, 2025. Credit: Doug Hardy / CTNewsJunkie WASHINGTON – US Sen. Richard ...

a hit to his reputation and a decrease in his brand's value before his contract renegotiation with the record label this year. The suit added that UMG "understood the recording's inflammatory and ...